scholarly article | Q13442814 |
P8150 | COVIDWHO ID | covidwho-1966 |
P6179 | Dimensions Publication ID | 1125089278 |
P356 | DOI | 10.1038/S41564-020-0688-Y |
P953 | full work available at URL | https://www.nature.com/articles/s41564-020-0688-y |
P932 | PMC publication ID | 7095430 |
P698 | PubMed publication ID | 32094589 |
P8299 | Semantic Scholar corpus ID | 211253784 |
P50 | author | Michael Letko | Q89866687 |
Vincent J. Munster | Q37375884 | ||
Andrea Marzi | Q50285805 | ||
P2860 | cites work | A transmembrane serine protease is linked to the severe acute respiratory syndrome coronavirus receptor and activates virus entry | Q24306622 |
Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC | Q24329089 | ||
Severe acute respiratory syndrome coronavirus-like virus in Chinese horseshoe bats | Q24536078 | ||
Conformational reorganization of the SARS coronavirus spike following receptor binding: implications for membrane fusion | Q27302420 | ||
Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus | Q28188496 | ||
Bats are natural reservoirs of SARS-like coronaviruses | Q28274751 | ||
Isolation and characterization of a bat SARS-like coronavirus that uses the ACE2 receptor | Q30219701 | ||
Proteolytic activation of the SARS-coronavirus spike protein: cutting enzymes at the cutting edge of antiviral research. | Q30354466 | ||
Further Evidence for Bats as the Evolutionary Source of Middle East Respiratory Syndrome Coronavirus | Q30400728 | ||
Efficient activation of the severe acute respiratory syndrome coronavirus spike protein by the transmembrane protease TMPRSS2. | Q30432156 | ||
Protease-mediated enhancement of severe acute respiratory syndrome coronavirus infection | Q30447031 | ||
Cleavage of the SARS coronavirus spike glycoprotein by airway proteases enhances virus entry into human bronchial epithelial cells in vitro | Q33516234 | ||
Structure, Function, and Evolution of Coronavirus Spike Proteins | Q33760875 | ||
Receptor usage and cell entry of bat coronavirus HKU4 provide insight into bat-to-human transmission of MERS coronavirus | Q34120263 | ||
Structure of SARS coronavirus spike receptor-binding domain complexed with receptor | Q34451350 | ||
Molecular diversity of coronaviruses in bats. | Q34519162 | ||
Vesicular stomatitis virus-based Ebola vaccines with improved cross-protective efficacy | Q34632946 | ||
Replication and shedding of MERS-CoV in upper respiratory tract of inoculated dromedary camels | Q34641515 | ||
Differential sensitivity of bat cells to infection by enveloped RNA viruses: coronaviruses, paramyxoviruses, filoviruses, and influenza viruses | Q34983662 | ||
Cleavage and activation of the severe acute respiratory syndrome coronavirus spike protein by human airway trypsin-like protease | Q35599437 | ||
Host cell proteases: Critical determinants of coronavirus tropism and pathogenesis | Q35735214 | ||
A pneumonia outbreak associated with a new coronavirus of probable bat origin | Q84367633 | ||
Rousettus aegyptiacus Bats Do Not Support Productive Nipah Virus Replication | Q91089778 | ||
Trypsin Treatment Unlocks Barrier for Zoonotic Bat Coronavirus Infection | Q91697408 | ||
Receptor Recognition by the Novel Coronavirus from Wuhan: an Analysis Based on Decade-Long Structural Studies of SARS Coronavirus | Q93037598 | ||
Two Mutations Were Critical for Bat-to-Human Transmission of Middle East Respiratory Syndrome Coronavirus | Q35913859 | ||
SARS-CoV infection in a restaurant from palm civet | Q36009490 | ||
RNA recombination in a coronavirus: recombination between viral genomic RNA and transfected RNA fragments | Q36702356 | ||
A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence | Q36702376 | ||
A system for functional analysis of Ebola virus glycoprotein | Q36831630 | ||
Synthetic recombinant bat SARS-like coronavirus is infectious in cultured cells and in mice | Q36986417 | ||
Activation of the SARS coronavirus spike protein via sequential proteolytic cleavage at two distinct sites | Q37138587 | ||
Recombination, reservoirs, and the modular spike: mechanisms of coronavirus cross-species transmission | Q37631303 | ||
Discovery of a rich gene pool of bat SARS-related coronaviruses provides new insights into the origin of SARS coronavirus | Q46251133 | ||
Newly discovered coronavirus as the primary cause of severe acute respiratory syndrome. | Q51660929 | ||
Adaptive Evolution of MERS-CoV to Species Variation in DPP4 | Q56557651 | ||
Attenuation of replication by a 29 nucleotide deletion in SARS-coronavirus acquired during the early stages of human-to-human transmission | Q57477156 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | angiotensin I converting enzyme 2 | Q301630 |
viral entry into host cell | Q4118894 | ||
Betacoronavirus | Q16532287 | ||
COVID-19 | Q84263196 | ||
Coronavirus spike protein | Q108250944 | ||
virus receptors | Q66053321 | ||
SARS-CoV-2 | Q82069695 | ||
P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
P304 | page(s) | 562-569 | |
P577 | publication date | 2020-02-24 | |
P1433 | published in | Nature Microbiology | Q23022567 |
P1476 | title | Functional assessment of cell entry and receptor usage for SARS-CoV-2 and other lineage B betacoronaviruses | |
P478 | volume | 5 |
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